Variant (rsID / SNP)

rs149911093

rs149911093 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAL1. Location: chromosome 14, position 74,154,097. Clinical significance in the table: Benign.

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Reference-table entries

DNAL1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:74154097
Cytoband: 14q24.3
HGVS: NM_031427.4(DNAL1):c.391+9A>G
Allele change: Silent

Associated conditions / phenotypes

Primary ciliary dyskinesia 16

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.